A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045484



Internal ID19134703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7862523..7930290hg38UCSC Ensembl
Innerchr16:7912525..7980292hg19UCSC Ensembl
Innerchr16:7852526..7920293hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3867768
hg1967768
hg1867768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2721n100
Supporting Variantsnssv3557094
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045484
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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